A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519473



Internal ID15100080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73057625..73059727hg38UCSC Ensembl
Innerchr17:71053764..71055866hg19UCSC Ensembl
Innerchr17:68565359..68567461hg18UCSC Ensembl
Innerchr17:68565359..68567461hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg382103
hg192103
hg182103
hg172103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv689421, nssv687261, nssv656304
Samples
Known GenesSLC39A11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519473
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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